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Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/70371

Type: Journal article
Title: Comparative toxicity of polyglutamine, polyalanine and polyleucine tracts in Drosophila models of expanded repeat disease
Author: van Eyk, Clare Louise
McLeod, Catherine Jean
O'Keefe, Louise Veronica
Richards, Robert Ian
Citation: Human Molecular Genetics, 2012; 21(3):536-547
Publisher: Oxford Univ Press
Issue Date: 2012
ISSN: 0964-6906
School/Discipline: School of Molecular and Biomedical Science : Genetics
Statement of
Responsibility: 
Clare L. van Eyk, Catherine J. McLeod, Louise V. O'Keefe and Robert I. Richards
Abstract: Homopolymeric amino acid repeat sequences in proteins are of particular interest due to the discovery that expanded copy numbers of these repeats are the molecular basis for a growing list of human genetic diseases. Repeat copy numbers above a typical normal range of polyglutamine repeats have been found to be the principal pathogenic agents in a number of these diseases, including Huntington's disease. There is emerging evidence that expansions of amino acids encoded by other reading frames of CAG/CUG repeats, including polyalanine and polyleucine, could contribute to toxicity in the 'polyglutamine' diseases. We have therefore used the Drosophila model system to investigate effects of ectopic expression of polyglutamine, polyleucine and polyalanine repeats in vivo to assess their relative toxicities and the common and distinct characteristics of the pathogenesis that they cause. We find that these homopolymeric sequences all exhibit toxicity and are able to form aggregates in Drosophila, although there are marked differences in the degree of toxicity dependent upon the tissue in which they are expressed.
Rights: © The Author 2011
RMID: 0020116231
DOI: 10.1093/hmg/ddr487
Appears in Collections:Genetics publications
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